A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6518189



Internal ID20891550
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:3896601..3904500hg38UCSC Ensembl
chr20:3877248..3885147hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg387900
hg197900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18068874
Samples
Known GenesPANK2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6518189
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer